U.S. patent application number 12/453577 was filed with the patent office on 2009-11-19 for blood components separator disk.
This patent application is currently assigned to Harvest Technologies Corporation. Invention is credited to James R. Ellsworth, Steven F. Levesque.
Application Number | 20090283524 12/453577 |
Document ID | / |
Family ID | 22740538 |
Filed Date | 2009-11-19 |
United States Patent
Application |
20090283524 |
Kind Code |
A1 |
Ellsworth; James R. ; et
al. |
November 19, 2009 |
Blood components separator disk
Abstract
A separator disk for use in centrifugal separation of components
is designed to automatically position itself during separation at
the interface between the supernatant and the remaining components.
Preferably the interface is between plasma and red blood cells.
Inventors: |
Ellsworth; James R.;
(Marshfield, MA) ; Levesque; Steven F.; (Hanson,
MA) |
Correspondence
Address: |
CLARK & BRODY
1090 VERMONT AVENUE, NW, SUITE 250
WASHINGTON
DC
20005
US
|
Assignee: |
Harvest Technologies
Corporation
|
Family ID: |
22740538 |
Appl. No.: |
12/453577 |
Filed: |
May 15, 2009 |
Related U.S. Patent Documents
|
|
|
|
|
|
Application
Number |
Filing Date |
Patent Number |
|
|
11206869 |
Aug 19, 2005 |
7547272 |
|
|
12453577 |
|
|
|
|
10019680 |
Jan 4, 2002 |
7077273 |
|
|
PCT/US01/11732 |
Apr 27, 2001 |
|
|
|
11206869 |
|
|
|
|
60200150 |
Apr 28, 2000 |
|
|
|
Current U.S.
Class: |
220/216 |
Current CPC
Class: |
B01D 21/2433 20130101;
B01D 2221/10 20130101; B04B 11/00 20130101; B01D 17/0217 20130101;
B01L 3/5021 20130101; A61M 1/029 20130101; B01L 2300/0803 20130101;
B01D 21/26 20130101; A61M 1/3693 20130101; B04B 7/12 20130101; B04B
7/00 20130101; G01N 33/491 20130101; B01D 21/26 20130101; B01L
3/50215 20130101; B01D 21/2433 20130101; B01D 21/262 20130101; B01L
2300/0832 20130101 |
Class at
Publication: |
220/216 |
International
Class: |
B65D 51/00 20060101
B65D051/00 |
Claims
1-10. (canceled)
11. An article for use in preventing flow of a fluid from a tube,
said article being generally disk shaped and having a raised edge
portion such that the center of buoyancy of the article lies above
an upper surface thereof.
12-16. (canceled)
Description
TECHNICAL FIELD
[0001] This invention relates to methods and apparatus for use in
the separation of fluids into components having different specific
gravities. The invention finds particular utility in the
centrifugal separation of the components of blood.
BACKGROUND
[0002] Centrifugal separation of blood into components of different
specific gravities, such as red blood cells, white blood cells,
platelets, and plasma is known from U.S. Pat. No. 5,707,331
(Wells). The apparatus shown in that patent employs a disposable
processing tube having two chambers, and blood to be separated into
components is placed in one of the chambers. The processing tube is
placed in a centrifuge, which subjects the blood to centrifugal
forces to separate the components. The supernatant is then
automatically decanted into the second of the chambers.
[0003] To retain, principally, the red blood cells during the
decant of the supernatant, the apparatus disclosed in the Wells
patent includes a shelf placed in the first chamber at the expected
level of the interface between the red blood cells and the
less-dense components, including the plasma. One problem with the
arrangement shown in the '331 Wells patent, however, is that the
position of the interface varies with the particular proportions of
the components (e.g., the hematocrit) of the blood to be processed.
Thus, if the shelf is placed at the expected position of the
interface for blood of average hematocrit, and the hematocrit of
the particular blood being processed is low, the shelf will be
above the interface after separation. Such a position of the shelf
will hinder the flow of the components near the interface during
decanting, thus retaining significant amounts of these components
in the first chamber and reducing the separation efficiency of the
system.
SUMMARY OF THE INVENTION
[0004] In accordance with the invention, a movable separator disk,
which automatically positions itself at the interface between the
separated components, is placed in the first chamber. In the
preferred embodiment, the disk is capable of moving vertically and
is designed to position itself automatically at the interface
between red blood cells and the remaining components in the
centrifugal separation of blood.
[0005] Decant of the supernatant can be either by gravity drain or
by centrifugal transfer, and a main function of the disk is to
restrict the flow of the component below it, e.g., red blood cells,
during decant. This ensures that the supernatant is not
contaminated and increases the efficiency of the process.
[0006] The invention contemplates two embodiments for the disk. In
one embodiment, the disk is supported on a central shaft such that
an annulus is formed between the perimeter of the disk and the
interior surface of the first chamber. The dimensions of the
annulus are such that the flow of red blood cells through it during
decant is restricted such that they do not contaminate the decanted
supernatant to any significant degree.
[0007] In another embodiment, the disk is arranged on the shaft
such that, when the chamber is tilted for gravity decanting, the
disk rotates such that one edge of the disk engages the wall of the
chamber to block flow of red blood cells.
[0008] In either of these embodiments, the specific gravity of the
disk and its shape may be chosen so that a major part of the upper
surface lies just below the interface, thus facilitating release of
the supernatant from the disk during decanting. This upper surface
is also preferably curved to match the cylindrical shape the
interface assumes during centrifugation.
BRIEF DESCRIPTION OF THE DRAWINGS
[0009] FIG. 1a is a longitudinal cross-section of a portion of a
processing tube chamber and a separator disk in accordance with a
first embodiment of the invention.
[0010] FIG. 1b is a transverse cross section taken along line 1b-1b
of FIG. 1a.
[0011] FIG. 2a is a longitudinal cross-section of the embodiment of
FIGS. 1a and 1b when the separator disk is tilted during
decanting.
[0012] FIG. 2b is a transverse cross section taken along line 2b-2b
of FIG. 2a.
[0013] FIG. 3a is a longitudinal cross-section of a second
embodiment of the invention.
[0014] FIG. 3b is a transverse cross section taken along line 3b-3b
of FIG. 3a.
[0015] FIG. 4 is a longitudinal cross-section of a third embodiment
of the invention.
DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS
[0016] With reference to FIGS. 1 and 2, one chamber 2 of a
processing tube, such as that shown in the '331 Wells patent has a
separator disk 4 in accordance with the invention supported therein
by a central shaft 6. The shaft 6 is designed to direct fluid
introduced into the chamber to the bottom of the chamber. This
precludes the formation of an air bubble at the bottom of the
chamber, particularly when the bottom of the chamber is tapered.
Thus, fluid is introduced into the chamber by inserting a cannula
attached to a syringe containing blood into the shaft 6 and
discharging the blood from the syringe into the chamber. A central
opening 8 in the disk receives the shaft 6 in such a manner that
the disk easily slides along the shaft.
[0017] The shaft 6 may not be necessary in all instances, for
example, when the bottom of the processing tube is flat. In that
instance the disk does not have a central hole.
[0018] The disk is preferably made of material having a specific
gravity that allows the disk to float at the interface with red
blood cells. In the preferred embodiment that specific gravity is
about 1.04 (e.g., polystyrene), which is just less than the
specific gravity of red blood cells at 70% hematocrit. Thus, when
the blood is centrifuged, the disk moves to the interface between
the red blood cells and the other components.
[0019] The interface will naturally assume a cylindrical shape with
a cylindrical radius equal to the distance to the center of
rotation of the centrifuge. The disk may be cylindrical, to match
the shape of the interface.
[0020] In the embodiment shown in FIGS. 1a, 1b, 2a and 2b, the
diameters of the hole 8 and the shaft 6 are such that an annular
gap 10 is formed between the outer surface of the shaft and the
interior surface of the hole 8. Similarly, an annular gap 12 is
provided between the perimeter of the disk and the interior surface
of the tube 2.
[0021] FIGS. 1a and 1b illustrate the position of the disk during
centrifugation, and it will be appreciated that the gaps 10 and 12
are large enough to allow passage of the descending heavier
components, e.g., red blood cells and the ascending lighter
components, e.g., plasma. According to this embodiment, however,
the diameter of the central opening 8 is large enough whereby
during decanting the disk 4 rotates as shown in the figures. Thus,
when the processing tube is rotated to the decant position, the
more dense red blood cells, illustrated at 14, that have
accumulated below the disk exert a force against the bottom of the
disk as they try to flow through the gap 12. This causes the disk 4
to rotate, as shown in FIGS. 2a and 2b, until a portion of the
lower outer edge 16 of the disk and also the upper outer edge 18
engage the inner surface of the chamber 2. This engagement between
the edge 16 of the disk and the interior of the chamber effectively
forms a valve that prevents flow of the red blood cells, allowing
decant of the plasma supernatant without contamination by red blood
cells. It will be appreciated that this embodiment requires the
transverse dimension of the disk between edges 16 and 18 to be
greater than the internal diameter of the tube so that the edges
engage the interior of the tube when tilted.
[0022] A second embodiment is shown in FIGS. 3a and 3b. According
to this embodiment, the gap 10 is made to be small whereby the disk
does not rotate appreciably during decant, in contrast to the
embodiment of FIGS. 1 and 2. It will be appreciated that an annular
channel is formed by the gap 12, this channel having a width equal
to the radial dimension of the gap and a length equal to the
thickness of the disk at the edge. The rate of flow of a fluid
through this channel is a function of the dimensions of the
channel, and the dimensions of the disk of this embodiment are such
that the red blood cells will not flow appreciably through the
channel at 1 G. In the preferred embodiment, the width of the gap
is about 0.005 inch to about 0.020 inch, and the length is about
0.1 inch to about 0.3 inch.
[0023] Thus, the components of the blood flow through the channel
during centrifugation (i.e., at 1000 G), but do not flow
appreciably through the channel during decanting at 1 G. This
allows the supernatant to be decanted without significant
contamination by the red blood cells.
[0024] FIG. 4 illustrates a preferred shape of the disk 4. In this
embodiment, the top surface 20 of the disk is concave, preferably
cylindrical, and the disk is provided with an elongated central
portion 22. The specific gravity of the disk material is selected
so that the concave surface 20 is located just below the interface.
That is, the thickness of the outer edge, the length of the portion
22, and the specific gravity of the material are chosen so that the
center of buoyancy of the disk is just above the concave surface,
and that surface will be just below the interface 26 with red blood
cells. This arrangement allows a small layer 24 of the red blood
cells to form on the upper surface.
[0025] The layer of red blood cells 24 reduces the surface tension
between the platelets at the interface 26 and the surface 20 of the
disk and facilitates release of the platelets from the disk. This
is important to ensure that all of the platelets are decanted, and
the small amount of red blood cells that may be decanted along with
the supernatant does not generally represent a significant
contamination of the supernatant.
[0026] Modifications within the scope of the appended claims will
be apparent to those of skill in the art.
* * * * *